The minimal expression of non-synonymous mutations inside our KPC magic size and having less predicted neo-epitopes in a position to bind MHC class I (n=0C5 predicted neo-epitopes per tumor; unpublished data) suggests the prospective peptide-MHC tumor repertoire can be mechanistically specific from that root responsiveness to checkpoint blockade
The minimal expression of non-synonymous mutations inside our KPC magic size and having less predicted neo-epitopes in a position to […]